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Sep-tek.Ch.11 (continued)
Distillation (Multistage with reflux)Sigurd Skogestad
Distillation• Separation of liquid mixtures by repeated evaporation
– multi-stage with reflux– Old name: ”Rectification”
• Basis: Components have different boiling points (different volatility)• Most common separation process in industry
– Chemicals– Oil and gas
• ”Separating agent” = heat (thermal energy)• 3% of world energy consumption is for distillation
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When use distillation?• Liquid mixtures (with difference in boiling point)• Unbeatable for high-purity separations because
• Essentially same energy usage independent of (im)purity!» Going from 1% to 0.0001% (1 ppm) impurity in one product increases energy usage only by about 1%
• Number of stages increases only as log of impurity!» Going from 1% to 0.0001% (1 ppm) impurity in one product increases required number of stages only by factor 3 (Proof using Fenske:
ln(1.e-6)/ln(1.e-2)=3)
• Well suited for scale-up» Columns with diameters over 18 m
• Examples of unlikely uses of distillation: » High-purity silicon for computers (via SiCl3 distillation)» Water – heavy-water separation (boiling point difference only 1.4C)
Sigurd and distillation• 1980-83 (Norsk Hydro): Steady-state design and simulation
– Crude oil, Mongstad refinery– Petrochemicals, VCM– Methanol-water, formic acid-water– Mostly thermodynamics
• 1983-rest of life: Control and dynamics• 1995-2000: Optimal batch (multivessel)• 1997-present: Optimal integrated continuous distillation columns (Petlyuk, Kaibel)• http://www.nt.ntnu.no/users/skoge/distillation/
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F
V
L
B
D
Bottom section
Top section
CONTINOUS DISTILLATION
I prefer to number the stagesfrom the bottom (with reboiler=1), BUT the book does it from the top.
(I prefer numbering from bottom, like in a building, because this makes more sense if theequlibrium stage is a physical tray)
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Alternative: Packed column
Trayed column:
Both cases: Want intensive mixing and large surface area between phases
Lab
Packed Tray Tray
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Distillation column modeling• Equlibrium stage concept: Many flashes on top of each other!• Each stage is an adiabatic flash:
– Component balance– Energy balance– Vapor-liquid equilibrium (VLE), y = K x
1. Detailed numerical solution is straightforward but requires computer• Commercial: Unisim / Hysys, Aspen• Free software (very nice!): ChemSep.org
2. Analytical solution– Possible is certain cases– Most common assumption: Constant molar flows (simplified energy balance)
• Constant K (VLE) + constant molar flows: Kremser-equations• Constant relative volatility (VLE) + constant molar flows: Fenske, Underwood.
3. Graphical solution• Graphical solution of component balances + VLE• Any VLE + Constant molar flows: McCabe-Thiele
Stage n
Stage n-1
Stage n+1
Vnyn
Vn+1yn+1
Ln-1Xn-1
Lnxn
Equilibrium (VLE): yn = fn(xn,…)
Vn-1yn-1
Material balance stage i (out=in)*:Ln xn + Vn yn = Ln-1xn-1 + Vn+1yn+1
The equilibrium stage concept
Note: Numbering is here from top (as in book).
* We usually make balances to end of column. Gives same result!
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B, xB
Top section
Btm section
Top operating line. Goes through point (xD,XD) and has slope LT/VT<1.Proof: x=xD gives: y = (LT+D)xD/VT = xD
y
yx
xVT LT
Top operating line:y and xbetween stagesin top section
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yB
B, xB
Bottom operating line. Goes through point (xB,xB) and has slope LB/VB>1.
VBLB
y x
Bottom operating line:y and x between stagesin bottom section
LB = LT + qF VT = VB+ (1-q)Fq = Fraction of liquid in feed
T=top section
B=btm section
4. Feed line (crossing of operating lines):
Proof:Top: VT y = L T x + D xDBot tom: VB y = L B x ¡ B xBAt crossing of these lines, y and x are same. Subt ract :y (VT ¡ VB )| { z }
(1¡ q)F= x (L T ¡ L B )| {z }
¡ qF+ F xF
) y = ¡ q1¡ q x + x F1¡ q (feed line)
y and x forintersection of operating lines
Liquid feed
Vapor feed
Subcooled liquid feed
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Usually: Constant molar flows assumption
• Each section: Constant molar flows of liquid L and vapor V:– VT = V1 = V2 = Vn =Vn+1 – LT = L1 = L2 = Ln = Ln+1 = L– VB = VN = Vm =Vm+1 – LB = LN = Lm =Lm+1
• Replaces energy balance– Holds for components with similar heat of vaporization
Top
Btm
" Operat ing line" = Relat ionship between y and x between stages (from materialbalance).Top sect ion: y = L TVT x + DVT xDBtm sect ion: y = L BVB x ¡ BVB xBCrossing (feed line): y = q
q¡ 1 x ¡ x Fq¡ 1
, Total balance at feed: L B = L T + qF , VT = VB + (1 ¡ q)F
Summary operating lines for Constant molar flows
cooling
heating
F
D
BVB
VT
LB
LTq = Fraction liquid in feed
Goes through (y,x)=(xD,xD) + (y,x)=(DxD/VT,0)=(xD/(R+1),0)Goes through (y,x)=(xB,xB) + crossing of top/feed-linesGoes through (y,x)=(xF,xF) + has slope q/(q-1)
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McCabe-Thiele graphical methodExample: Benzene-Toluene continuous distillation
• F = 100 kmol/h• xF = 0.45, qF =1.19 (subcooled liquid)• Desired products: xD=0.95, xB=0.1• Given: R= LT/D = 4• How many stages are required?
• x,y – mole fractions bemzene (light component)
B, xB
Top section
Btm section
LT
LB
VB
VT
VB
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McCabe-Thiele graphical solution0. Use overall mass balances to find product compositions, product flows and flows inside column.1. Draw equilibrium curve: (x,y) on stages.2. Draw upper operating line: (x,y) between stages.
Starts in (xD,xD) and has slope LT/VT = R/(R+1) where R=L/D. Goes through (x,y)=(0,xD/(R+1))=(0, 0.19)3. Draw feed lines (goes through (xF,xF) and has slope –q/(1-q).
• Feed sat. liquid (q=1): Vertical. • Feed sat. vapor (q=0): Horizontal• Partly vapor (0<q<1): Between (negative slope)• Feed subcooled (q>1): Positive slope (see Figure below)
4. Draw lower operating line : (x,y) between stages. Starts in (xB,xB) and goes through crossing of feed line and upper operating line5. Graphical solution to find number of stages: Start from product and switch between on stages (xn,yn) and between stages (xn,yn+1) by making staircase.6. Optimal feed location (design): Switch between operating lines at feed line (=crossing of operating lines)7. Given N and NF (more difficult): Need to guess product composition and iterate to fit in N stages
(x1,y2)
(x1,y1)
(x2,y3)
(x2,y2) (xD,y1) = (xD,xD) tot. condenser
Note: This feed (q) line is for subcooled liquid feed (q>1)
(0,0.19)
xB
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1
3.6
23 To find no. of stages in each section:
Often easier to start from both ends.Let final stairs reach crossing (xF*,yF*)
Counting from top to feed: 4.1 stagesCounting from btm to feed: 3.6 stagesTotal: 7.7 stages
Previous slide:Counting from top to btm: 7.6 stages
No. of stages in each section
(xF*,yF*) = crossing = optimal feed stage composition
If “too many” stages in top section:Get “pinch zone” above feed
“Pinch zone” = zone with small change in composition
1. Nonoptimal feed stage locationSome comments on distillation and McCabe-Thiele
Comments:1. Exact location of feed stage is not critical unless the column is poorly designed
with “too few” stages2. Existing column: During operation, one may get non-optimal feed location (with
pinch) because of changes in feed composition and product purities.
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2. Reboiler and condenser duty• Reflux: L = LT• Assuming constant molar flows:
LB = L + qF VB = LB – B = L + qF – BVT = VB + (1-q)F = L + D
• Reboiler and condenser duty• QB [J/s]= VB [mol/s] ·ΔHBvap [J/mol]• QC [J/s]= VT [mol/s] ·ΔHDvap [J/mol] (total condenser)• Note: If feed is liquid & total condenser: QB ¼ QC.
Example: L=LT=(L/D)*D=4*41.17 = 164.68 kmol/h, VB = L + qF – B = 164.68 + 1.19*100 – 58.83 = 224.85 kmol/hQB = VB ·ΔHBvap = 224.85*(1000/3600)*32.1*1000 J/s = 2.0 e6 J/s = 2.0 MW
3. Minimum number of stages, Nmin(with total reflux, that is, infinite energy)A. Graphical
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3. Minimum no. of stages, Nmin ( with total reflux)• Assumption VLE: Constant relative volatility. Stage i (L=light component, H = heavy component):
• Repeat for all N stages
• Fenske’s formula for minimum no. of stages
• Applies also to column sections• Example. Benzene-Toluene.
Stage i
Stage i+1Viyi
Vi-1yi-1
Li+1xi+1
Lixi
Total reflux:Vi = Li+1yi = xi+1
B. Analytical (constant )
Number of stages increases only as log of impurity!
• Example: α=2. Binary separation with purities: 90% light in top and 90% heavy in bottom:
• Example: α=2. Binary separation with purities: 99.9% light in top and 98% heavy in bottom:
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CommentsNumber of stages• Reboiler (“partial reboiler”): Gives 1 theoretical stage• Total condenser: 0 stage• Partial condenser: 1 theoretical stage• N is usually (e.g., in Fenske’s fomula, N = lnS/lnα) the total no. of theoretical stages including reboiler and partial condenser• Thus: Nstages inside column = N-1 (or N-2 for partial condenser)
“Total reflux” vs. “Total condenser”We use "total" with (at least) two different meanings:1."Total condenser" = all is condensed (so D is liquid)2."Total reflux" = (all is condensed and) all is send back as reflux (so D=0 or more generally L>>D)
4. Minimum reflux (minimum energy)(with infinite number of stages)
Nonideal mixture:A. Graphical
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• King’s formula, assuming pinch at feed (not in book):
4. Minimum reflux (minimum energy)(with infinite number of stages)
B. Analytical (constant )
NOT IN BOOK
•Note: Essentially same energy usage independent of (im)purity!Pure products:
Easy to remember!
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5. Design: “Optimum” reflux or How many stages (N)?
5A. Energy (V) vs. number of stages (N)• Trade-off between number of stages and energy
• Actual V approaches Vmin for N approximately 2 x Nmin or larger, typically:
N=2Nmin Vmin + 25% N=3Nmin Vmin + 3 % N=4Nmin Vmin + 0.3 %Energy
Numb
er of st
ages
Vmin
Nmin
Conclusion:Recommend N= 2.5 Nmin (use higher value to save energy and simplify operation).
Gives actual boilup (energy) V ¼ 1.1 Vmin
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10.6B Equipment for absorption and distillation
Random/dumped packings
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Structured packing (1970’s)
Structured packings (today)
Mellapak (Sulzer)Koch-Glitsch
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6. Height of real columns (section 11.5) • N = no. of theoretical stages (total)• Ninside = no. of theoretical stages inside column
= N - 1 (total condenser, assuming reboiler gives 1 theoretical stage)= N – 2 (partial condenser)
– Tray columns:• Ntrays = Actual number of trays inside column• Eo=overall tray efficiency (typical 0.7)• Ntrays = Ninside / EoComment: Sigurd does not recommend using Murphy or Point efficiency
– Packed columns: • H = height of packings [m] = Ninside* HETP• HETP = height equivalent to 1 theoretical plate• Estimation of HETP:
1. Mass transfer modelHETP ¼ H0G * f = f * V / (Ky a S) (10.6-55) (not very reliable, f = ln(1/A)/(1/A-1))2. Rule of thumb (recommended in practice)
– Random packing: HETP [m] = 18 Dp [m] (equation 11.5-11)Dp = diameter of each packing element
3. (Best) Data from packing manufacturer
7. Column operation and diameter
flooding
Similar for packed column
Packed:Channeling / packing not wetted Liquid buildup
Liquid load
Gas load
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Column diameter• In many cases the diameter is determined by the
(superficial) gas velocity v [m/s]v[m/s] = V[m3/s] / A[m2]Where for ideal gas: V[m3/s] = V[mol/s] · RT/p
• Example. Column at 2 bar with V = 50 mol/s and given vmax = 1.5 m/s. Temperature bottom (highest) = 400K.– Then V [m3/s] = 50 mol/s · 8.31 J/K,mol · 400K /2.e5 Pa = 0.83 m3/s– A [m2] = V[m3/s] / vmax [m/s] = 0.83 / 1.5 = 0.553 m2– Column area A = (π/4) D2– Conclusion: Diameter D = √(4A/π) = √(4· 0.553 / 3.14) = 0.84 m
Trayed column• Maximum vapor velocity is limited by entrainment• Tray column. Fair correlation:
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Packed column• Maximum gas load limited by flooding
Flooding, gives vmax
8. Trays vs. packings• Packings:
+ Much smaller pressure drop (typically 1/10)+ Usually: More stages for given column height- Problems with liquid distribution in larger columns (can use structured packings, but more expensive)
• Trays:+ More easy to clean+ Better for large capacity columns+ Larger holdup (typically, 2 times larger): Advantage for control (“have more time”)- Can have inverse response in bottom of column (- effect - difficult to predict)
• Overall: Differences are surprisingly small – also for process control
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9. Special cases of distillation1. Stripping column (no top part)2. Enriching column (no btm part)3. Stripper / absorber (no condenser or reboiler)4. ”Direct” steam injection (instead of heat)5. Column with side stream6. Partial condenser (gives 1 extra eq. stage)7. More than one feed
• All cases: Exactly same principles (can use McCabe-Thiele)• Start with material balances to derive operating lines• Need equilibrium data!
10. Multicomponent mixtures• Most of the derivations apply to the multicomponent case• Identify ”key components” (light and heavy, L-H) for split• McCabe-Thiele: Plot xy-diagram for pseudo-binary, x = xL/(xL+xH)• Fenske’s formula OK: Nmin = lnS / ln .
= relative volatility between L and HS = separation factor between L and H
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11. Shortcut: ”How to design a distillation column in 5 min”
1. Multicomponent: Identify key components (LH)2. Estimate relative volatility . Can use Sigurd’s formula*3. Find split (D/F) from desired product purities4. Stages (height of column): Find Separation factor S and Nmin = lnS / ln . Select N = 2.5 Nmin5. Feed stage: Can use another Sigurd-formula (last slide)6. Reflux / Energy usage: Find Lmin=F/(-1) (feed liquid) and Vmin/F. Real V is about 10% higher7. Diameter: A = (V[mol/s]RT/p ) / vmax. D = √(4A/π). Typical value: vmax= 2m/s.
*Sigurd’s formula
Example: “5 min column design”• Design a column for separating air• Feed: 80 mol-% N2 (L) and 20% O2 (H)• Products: Distillate is 99% N2 and bottoms is 99.998% O2• Component data
– Nitrogen: Tb = 77.4 K, Hvap=5.57 kJ/mol– Oxygen: Tb = 90.2 K, Hvap=6.82 kJ/mol
• Problem: 1) Estimate . 2) Find split D/F. 3) Stages: Find Nmin and 4) suggest values for N and NF. 5) Energy usage: Find Vmin/F for a) vapor feed and b) liquid feed. • Given: For vapor feed and sharp sep. of binary mixture: Vmin/F = 1/(-1)
IDEAL MIXTUREIDEAL VLE (constant α)
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Solution “5-min design”Also see paper (“Theory of distillation”)
IDEAL MIXTUREIDEAL VLE (constant α)
IDEAL MIXTUREIDEAL VLE (constant α)
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IDEAL MIXTUREIDEAL VLE (constant α)
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11. Distillation design in practice: Numerical solution using “simulators”.Example using Chemsep
• http://www.chemsep.org/• Written by Ross Taylor, Clarkson University• Lite version:
– max 50 stages and 5 components– free and extremely simple to use
• Example 11.4-2: Benzene-Toluene– Specify 8 stages, feed on stage 5 from top– Specify product compositions, xD=0.95, xB=0.10– Find: Reflux ratio L/D (was 4 but then we needed only 7.6 stages)
Enter title….Use arrow to go through menus
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Data input... components
... column configuration
Note: Program counts condenser as stage 1even if it is not an equlibrium stage
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... thermodynamics
Here: Raoults law + idea enthalpy Normally use:- Soave-RK equation of state (EOS) for relatively ideal mixtures like hydrocarbons- Gamma-Phi (UNIQUAC, SRK) for non-ideal components
... feed data
Can write 1atm and program converts automatically
Note: Use 55 mol/s (instead og 55 kmol/h)
Normally choose “Split”, but does not matter heresince the feed is subcooled
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Assume constant pressure (1 atm) in column(Normally the pressure drop is about 0.1 bar from the bottom to the top)
Assume 100% stage efficiency
Assume no heat loss
TOP: Specify xD=0.95 BTM: Specify xB=0.1
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Press solve…
… results… Streams
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McCabe-Thiele diagram23
45
6
9=reboiler
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Profiles
Before R= 4. Now we need less reflux (and less energy)because we have more stages (increased from 7.6 to 8)
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Liquid phase composition
x
Stage
TOP
BTM
toluene
benzene
Vapor phase composition
y
Stage
TOP
BTM toluene
benzene
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Flow profiles
Stage
Flows
VL
BTM
TOPNote: Not quite constant molar flowsbecause dHvap is different for components
Temperature profile
Temperature [K]
Stage
TOP
BTM
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Log (xL/xH)-plot (“key ratio profile”): Use to check feed location
log(xL/xH) straight line: Feed placement OK
Stage
BTM
TOP
Relative volatility
Stage
2.4 2.5 2.6
BTM
TOP
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1. More literature on distillation• King (Wiley, 1980) on distillation design• Shinskey (McGraw-Hill, 1984) on distillation control• Kister (McGraw-Hill, 1990) on distillation operation
• General info: http://lorien.ncl.ac.uk/ming/distil/distil0.htm
• I.J. Halvorsen and S. Skogestad, ``Distillation Theory'', In: Encyclopedia of Separation Science. Ian D. Wilson (Editor-in-chief), Academic Press, 2000, pp. 1117-1134.
• S. Skogestad, Dynamics and control of distillation columns - A tutorial introduction., Trans IChemE (UK), Vol. 75, Part A, Sept. 1997, 539-562 (Presented at Distillation and Absorbtion 97, Maastricht, Netherlands, 8-10 Sept. 1997).
• More: see home page Sigurd Skogestad http://www.nt.ntnu.no/users/skoge/http://www.nt.ntnu.no/users/skoge/distillation
• Free steady-state distillation software with thermo package : http://www.chemsep.org/
Extra slides
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Simple formula for feed stage location (Skogestad, 1987)
Example. C3-splitter. zFL=0.65, xDH= 0.005, xBL=0.1, =1.12.
IDEAL MIXTUREIDEAL VLE (constant α)
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